• Develop high-quality, engaging content including blog posts, articles, whitepapers, case studies, and social media updates that align with our brand voice and marketing goals. • Implement SEO best practices to optimize content for search engines and improve organic search rankings. • Collaborate with the marketing team to create and execute content strategies that attract and convert target audiences. • Monitor and analyze content performance using tools like Google Analytics, and make data-driven decisions to improve engagement and conversion rates. • Work closely with cross-functional teams, including design, product, and sales, to ensure content aligns with overall marketing objectives. • Manage and grow our social media presence across various platforms, ensuring consistent and engaging communication with our audience.

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Associate Director, Medical Writing is responsible for contributing to the medical writing portfolio within the clinical and regulatory areas. This includes authoring briefing documents, clinical trial medical synopses, protocols, investigator’s brochures, PIPs, CSRs, Health Authority briefing books, Health Authority responses, and other clinical documentation to support the conduct of trials and regulatory submissions/filings. The Associate Director participates in the development of templates and the establishment of medical writing processes and standards to ensure the quality and timeliness of regulatory filings and clinical documentation, in accordance with relevant regulatory guidelines and requirements. The Associate Director proactively leads departmental activities and various process improvement initiatives, and shares insights from lessons learned. Document Creation and Review: - Independently author and review complex clinical and regulatory documents, including clinical trial protocols, clinical overviews, and summaries in CTD/eCTD format for regulatory submissions. - Draft and edit more strategic documents, such as Health Authority briefing books, responses, and publications (abstracts, posters, slide presentations, and manuscripts for scientific journals). Team Leadership and Collaboration: - Represent medical writing on internal teams such as the Clinical Trial Team, protocol review committee, and regulatory submission teams. - Lead submission team activities and oversee the preparation of critical documents. - Facilitate team participation in document preparation, including scheduling meetings, developing timelines, and managing document reviews and decisions. - Act as a mentor for new employees and consultants and serve as a role model for junior writers. Process Development: - Lead the development and review of standard processes and templates. - Support ongoing improvements in cross-functional and global collaboration, sharing best practices and knowledge. Regulatory and Quality Adherence: - Maintain up-to-date knowledge of relevant regulatory guidelines and requirements. - Adhere to guidelines, SOPs, practices, and technical standards in all aspects of work. Professional Development: - Maintain current knowledge and competencies within relevant therapeutic and professional areas. - Contribute to knowledge sharing, skill-building, and good collaboration with stakeholders and colleagues. - Strategic thinker with a big-picture orientation. - Thorough, systematic, and organized. - Proactive, accountable, and goal oriented. - Innovative and a good team player. - Excellent at sharing knowledge and acting as a mentor. - Superior communication skills, capable of conveying scientific or medical information clearly and concisely. - Exceptional planning and coordinating abilities. - Ability to manage multiple tasks simultaneously. - Extensive knowledge of English grammar. - Expert in Microsoft 365. - Analytical skills with the ability to interpret and present clinical data and other complex information. Differentiated Skills: - Advanced leadership skills to guide and mentor team members. - Expertise in managing complex projects and submissions. - Strong influence and representation skills in high-level cross-functional teams. - Strategic vision to drive departmental goals and initiatives. - High level of knowledge of regulatory requirements and compliance. Communication and Interaction: - The role requires excellent oral and written communication skills to effectively present clinical results through scientific discussions, presentations, regulatory documents, and publications. - Close interaction with internal and external stakeholders, including various functions within Development Operations, project teams, regulatory bodies, medical and safety personnel, investigators, professional associations, consultants, and clinical research organizations. For US based candidates, the proposed salary band for this position is as follows: $160,080.00---$240,120.00 The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. When you join Genmab, you’re joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for: - 401(k) Plan: 100% match on the first 6% of contributions - Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance - Voluntary Plans: Critical illness, accident, and hospital indemnity insurance - Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave - Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support - Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses About You - You are genuinely passionate about our purpose - You bring precision and excellence to all that you do - You believe in our rooted-in-science approach to problem-solving - You are a generous collaborator who can work in teams with a broad spectrum of backgrounds - You take pride in enabling the best work of others on the team - You can grapple with the unknown and be innovative - You have experience working in a fast-growing, dynamic company (or a strong desire to) - You work hard and are not afraid to have a little fun while you do so! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com). Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

• Creating content that our audience will read and learn from. • Work with design, product, marketing, and sales to create the words that retain and attract customers • Shape (and scribe) our content strategy from newsletters, website copy, social media, and features pages • Communicate complex product benefits in ways that speak to our users and help them understand our products • Write using best practices for inclusivity and accessibility to reach users worldwide • Collaborate with our cybersecurity researchers to ensure their discoveries are easy to understand

• Oversee and lead the development of high-quality scientific documents, including clinical study reports, regulatory submission documents, publications, and other medical communications • Collaborate with cross-functional teams, including clinical, regulatory, and medical affairs teams, to ensure the delivery of accurate, clear, and well-structured documents that meet industry standards and regulatory requirements • Develop and oversee the preparation of clinical study reports (CSRs), clinical study protocols, investigator brochures, regulatory submission documents (e.g., INDs, NDAs), and other scientific/medical documents • Ensure the accuracy, clarity, and compliance of all documents with internal guidelines, industry standards, and regulatory requirements • Review and edit documents for consistency, style, and adherence to medical writing best practices • Support the preparation of regulatory submission documents and assist in the response to regulatory agency inquiries • Contribute to the preparation of scientific publications, abstracts, posters, and presentations for medical meetings • Implement and maintain efficient medical writing processes and tools to improve the quality and efficiency of document preparation • Ensure that all writing adheres to current guidelines, including ICH E6, ICH E3, GxP, and other relevant regulatory requirements • Provide detailed reviews and edits for accuracy, scientific content, grammar, style, and formatting • Provide training and development opportunities for junior writers, improving their skills in clinical and regulatory writing.